04633402

GUDID H981046334020

TI SNAP-ON OPEN PARALLEL CONNECTOR 6.0MM/6.0MM

Synthes GmbH

Bone-screw internal spinal fixation system, non-sterile
Primary Device IDH981046334020
NIH Device Record Keye6323b0f-9c65-4837-90dd-77bec76bf245
Commercial Distribution StatusIn Commercial Distribution
Version Model Number04.633.402
Catalog Number04633402
Company DUNS486711679
Company NameSynthes GmbH
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
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Phone+1(800)255-2500
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Phone+1(800)255-2500
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Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
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Phone+1(800)255-2500
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Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
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Phone+1(800)255-2500
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS110705034746760 [Primary]
HIBCCH981046334020 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWPAPPLIANCE, FIXATION, SPINAL INTERLAMINAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[H981046334020]

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[H981046334020]

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[H981046334020]

Moist Heat or Steam Sterilization


[H981046334020]

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[H981046334020]

Moist Heat or Steam Sterilization


[H981046334020]

Moist Heat or Steam Sterilization


[H981046334020]

Moist Heat or Steam Sterilization


[H981046334020]

Moist Heat or Steam Sterilization


[H981046334020]

Moist Heat or Steam Sterilization


[H981046334020]

Moist Heat or Steam Sterilization


[H981046334020]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2022-04-26
Device Publish Date2015-09-14

Devices Manufactured by Synthes GmbH

10886982349095 - NA2025-03-06 PLATE HOLDING FORCEPS LEFT FLARED TIPS
10886982349101 - NA2025-03-06 PLATE HOLDING FORCEPS RIGHT FLARED TIPS
10886982348265 - NA2025-03-05 XL IM REDUCTION TOOL CURVED WITH AO REAMER COUPLING
10887587078427 - NA2025-02-28 1.85MM ORTHOGNATHIC TAP
10886982344410 - NA2025-02-26 MAXFRAME CONTROL BOX TEMPLATE
10886982348333 - NA2025-02-26 1.1MM PARALLEL WIRE GUIDE
10886982348364 - NA2025-02-26 1.4MM PARALLEL WIRE GUIDE
10886982348395 - NA2025-02-26 1.6MM PARALLEL WIRE GUIDE

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